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Percent of clean cultures and percent of seed germination data were analysed against the seed capsule size and geographical location of the plant.
Monthly disease prevalence data were analysed against maximum temperatures for the periods of 7 and 14 days up to and including the sampling date, assuming a time lag in the corals' response to changing environmental parameters.
Data were analysed against the first day after harvest by one-way ANOVA, and means were compared using the Tukey test at α<0.05.
The sequencing data were analysed against the E. histolytica genome database (http://pathema.jcvi.org/cgi-bin/Entamoeba/PathemaHomePage.cgi) at the J. Craig Venter Institute using the Sequest algorithm (Eng et al., 1994) and also against the NCBI nr database.
The data were analysed against Dietary Reference Values for food energy and nutrients for the United Kingdom and observed intakes for the general population and for differences between IBS subtypes and the UK population.
The data were analysed against the UniProt database by means of the MASCOT algorithm (Matrix Science) using a precursor tolerance of 5 ppm, a fragment ion mass tolerance of 0.8 Da, one missed trypsin cleavage site and variable modifications.
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Data were analysed using a SI8000C analyser (Sony).
Our whole-exome data were analysed by filtering coding variants against dbSNP138, 1000Genomes, and NHLBI EVS Exome databases.
Data were analysed for variation in CF against HRV using linear regression and the Student's t test.
Data were analysed to determine vaccine efficacy against lesions attributable to vaccine HPV types (6, 11, 16, and 18) as well as to any tested HPV type, with the latter analyses including the 10 non-vaccine HPV types for which polymerase chain reaction testing was performed in protocols 013 and 015 (types 31, 33, 35, 39, 45, 51, 52, 56, 58, and 59).
Data were analysed using MASCOT software (Matrix Science), by searching against the Swiss-Prot/UniprotKB database.
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